Methods and apparatus for removing conductive material from a microelectronic substrate

ABSTRACT

A method and apparatus for removing conductive material from a microelectronic substrate is disclosed. One method includes disposing an electrolytic liquid between a conductive material of a substrate and at least one electrode, with the electrolytic liquid having about 80% water or less. The substrate can be contacted with a polishing pad material, and the conductive material can be electrically coupled to a source of varying electrical signals via the electrolytic liquid and the electrode. The method can further include applying a varying electrical signal to the conductive material, moving at least one of the polishing pad material and the substrate relative to the other, and removing at least a portion of the conductive material while the electrolytic liquid is adjacent to the conductive material. By limiting/controlling the amount of water in the electrolytic liquid, an embodiment of the method can remove the conductive material with a reduced downforce.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 10/665,219, now U.S. Pat. No. 7,112,122, entitled METHODS AND APPARATUS FOR REMOVING CONDUCTIVE MATERIAL FROM A MICROELECTRONIC SUBSTRATE, filed Sep. 17, 2003, which is incorporated herein in its entirety by reference. The present application relates to the following U.S. Patent Applications, all of which are incorporated herein in their entireties by reference: Ser. No. 09/651,779, now U.S. Pat. No. 7,074,113, filed Aug. 30, 2000; Ser. No. 09/888,084, now U.S. Pat. No. 7,112,121, filed Jun. 21, 2001; Ser. No. 09/887,767, now U.S. Pat. No. 7,094,131, filed Jun. 21, 2001; Ser. No. 09/888,002, now U.S. Pat. No. 7,160,176, filed Jun. 21, 2001, Ser. No. 10/230,970, now U.S. Pat. No. 7,220,166, filed Aug. 29, 2002; Ser. No. 10/230,972, now U.S. Pat. No. 7,134,934, filed Aug. 29, 2002; Ser. No. 10/230,973, now U.S. Pat. No. 7,153,195, filed Aug. 29, 2002; Ser. No. 10/230,628, now U.S. Pat. No. 7,078,308, filed Aug. 29, 2002; and Ser. No. 10/230,602, now U.S. Pat. No. 7,129,160.

TECHNICAL FIELD

This invention relates to methods and apparatuses for removing conductive material from microelectronic substrates.

BACKGROUND

Microelectronic substrates and substrate assemblies typically include a semiconductor material having features, such as memory cells, that are linked with conductive lines. The conductive lines can be formed by first forming trenches or other recesses in the semiconductor material, and then overlaying a conductive material (such as a metal) in the trenches. The conductive material is then selectively removed to leave conductive lines extending from one feature in the semiconductor material to another.

Electrolytic techniques have been used to both deposit and remove metallic layers from semiconductor substrates. For example, an alternating current can be applied to a conductive layer via an intermediate electrolyte to remove portions of the layer. In one arrangement, shown in FIG. 1, a conventional apparatus 60 includes a first electrode 20 a and a second electrode 20 b coupled to a current source 21. The first electrode 20 a is attached directly to a metallic layer 11 of a semiconductor substrate 10 and the second electrode 20 b is at least partially immersed in a liquid electrolyte 31 disposed on the surface of the metallic layer 11 by moving the second electrode downwardly until it contacts the electrolyte 31. A barrier 22 protects the first electrode 20 a from direct contact with the electrolyte 31. The current source 21 applies alternating current to the substrate 10 via the electrodes 20 a and 20 b and the electrolyte 31 to remove conductive material from the conductive layer 11. The alternating current signal can have a variety of wave forms, such as those disclosed by Frankenthal et al. in a publication entitled, “Electroetching of Platinum in the Titanium-Platinum-Gold Metallization on Silicon Integrated Circuits” (Bell Laboratories), incorporated herein in its entirety by reference.

One drawback with the arrangement shown in FIG. 1 is that it may not be possible to remove material from the conductive layer 11 in the region where the first electrode 20 a is attached because the barrier 22 prevents the electrolyte 31 from contacting the substrate 10 in this region. Alternatively, if the first electrode 20 a contacts the electrolyte in this region, the electrolytic process can degrade the first electrode 20 a. Still a further drawback is that the electrolytic process may not uniformly remove material from the substrate 10. For example, “islands” of residual conductive material having no direct electrical connection to the first electrode 20 a may develop in the conductive layer 11. The residual conductive material can interfere with the formation and/or operation of the conductive lines, and it may be difficult or impossible to remove with the electrolytic process unless the first electrode 20 a is repositioned to be coupled to such “islands.”

One approach to addressing some of the foregoing drawbacks is to attach a plurality of first electrodes 20 a around the periphery of the substrate 10 to increase the uniformity with which the conductive material is removed. However, islands of conductive material may still remain despite the additional first electrodes 20 a. Another approach is to form the electrodes 20 a and 20 b from an inert material, such as carbon, and remove the barrier 22 to increase the area of the conductive layer 11 in contact with the electrolyte 31. However, such inert electrodes may not be as effective as more reactive electrodes at removing the conductive material, and the inert electrodes may still leave residual conductive material on the substrate 10.

FIG. 2 shows still another approach to addressing some of the foregoing drawbacks in which two substrates 10 are partially immersed in a vessel 30 containing the electrolyte 31. The first electrode 20 a is attached to one substrate 10 and the second electrode 20 b is attached to the other substrate 10. An advantage of this approach is that the electrodes 20 a and 20 b do not contact the electrolyte. However, islands of conductive material may still remain after the electrolytic process is complete, and it may be difficult to remove conductive material from the points at which the electrodes 20 a and 20 b are attached to the substrates 10.

Another drawback with existing electrolytic methods is that they may not be suitable for removing certain conductive materials, including tantalum and tantalum compounds, from microelectronic substrates 10 at a high enough rate, or with the desired uniformity, while avoiding damage to the microelectronic-substrate. Accordingly, existing electrolytic methods may not be suitable for processing microelectronic substrates at production-level speeds.

SUMMARY

The present invention is directed toward methods and apparatuses for removing conductive materials from microelectronic substrates. A method in accordance with one aspect of the invention includes disposing an electrolytic liquid between an electrically conductive material of a microelectronic substrate and at least one electrode, with the electrolytic liquid having about 80% water or less. The microelectronic substrate is contacted with a polishing pad material and the conductive material of the microelectronic substrate is electrically coupled to a source of varying electrical signals via the electrolytic liquid and the at least one electrode. The method can further include applying a varying electrical signal to the conductive material, moving at least one of the polishing pad material and the microelectronic substrate relative to the other, and removing at least a portion of the conductive material from the microelectronic substrate while the electrolytic liquid is adjacent to the electrically conductive material.

In further aspects of the invention, the conductive material of the microelectronic substrate can include tantalum or a tantalum compound and the method for removing the conductive material can include moving at least one of the substrate and the at least one electrode relative to the other, without necessarily contacting the substrate with a polishing pad material. The method can further include complexing the tantalum as a metal-organic species in solution. The electrolytic liquid can include 1% water or less and the downforce applied to the microelectronic substrate can be about 1.0 psi or less. The method can further include at least restricting the amount of water in the electrolytic liquid.

An apparatus in accordance with an aspect of the invention includes an electrolytic liquid volume coupleable to a supply of electrolytic liquid, and a carrier positioned to releasably carry a microelectronic substrate in fluid communication with the electrolytic liquid volume. An enclosure can be disposed around the electrolytic liquid volume and the carrier, and can be configured to at least restrict the passage of water from a region external to the enclosure to a region internal to the enclosure. In further aspects of the invention, the enclosure can be coupled to a source of non-aqueous purge gas, and/or can include a support member configured to carry a polishing pad in contact with the microelectronic substrate.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a partially schematic, side elevational view of an apparatus for removing conductive material from a semiconductor substrate in accordance with the prior art.

FIG. 2 is a partially schematic side, elevational view of another apparatus for removing conductive material from two semiconductor substrates in accordance with the prior art.

FIG. 3 is a partially schematic, side elevational view of an apparatus having a support member and a pair of electrodes for removing conductive material from a microelectronic substrate in accordance with an embodiment of the invention.

FIG. 4 is a partially schematic, side elevational view of an apparatus for removing conductive material and sensing characteristics of the microelectronic substrate from which the material is removed in accordance with another embodiment of the invention.

FIG. 5 is a partially schematic, side elevational view of an apparatus that includes two electrolytes in accordance with still another embodiment of the invention.

FIG. 6 is a partially schematic, plan view of a substrate adjacent to a plurality of electrodes in accordance with still further embodiments of the invention.

FIG. 7 is a cross-sectional, side elevational view of an electrode and a substrate in accordance with yet another embodiment of the invention.

FIG. 8A is a partially schematic, isometric view of a portion of a support for housing electrode pairs in accordance with still another embodiment of the invention.

FIGS. 8B-8C are isometric views of electrodes in accordance with still further embodiments of the invention.

FIG. 9 is a partially schematic, side elevational view of an apparatus for both planarizing and electrolytically processing microelectronic substrates in accordance with yet another embodiment of the invention.

FIG. 10 is a partially schematic, partially exploded isometric view of a planarizing pad and a plurality of electrodes in accordance with still another embodiment of the invention.

FIG. 11 is a partially schematic, side elevational view of an apparatus for both planarizing and electrolytically processing microelectronic substrates in accordance with still another embodiment of the invention.

FIGS. 12A-B schematically illustrate a circuit and wave form for electrolytically processing a microelectronic substrate in accordance with yet another embodiment of the invention.

DETAILED DESCRIPTION

The present disclosure describes methods and apparatuses for removing conductive materials from a microelectronic substrate and/or substrate assembly used in the fabrication of microelectronic devices. Many specific details of certain embodiments of the invention are set forth in the following description and in FIGS. 3-12B to provide a thorough understanding of these embodiments. One skilled in the art, however, will understand that the present invention may have additional embodiments, or that the invention may be practiced without several of the details described below.

FIG. 3 is a partially schematic, side elevational view of an apparatus 160 for removing conductive material from a microelectronic substrate or substrate assembly 110 in accordance with an embodiment of the invention. In one aspect of this embodiment, the apparatus 160 includes a vessel 130 containing an electrolyte 131, which can be in a liquid or a gel state. A support member 140 supports the microelectronic substrate 110 relative to the vessel 130 so that a conductive layer 111 of the substrate 110 contacts the electrolyte 131. The conductive layer 111 can include metals such as platinum, tungsten, tantalum, gold, copper, or other conductive materials. In another aspect of this embodiment, the support member 140 is coupled to a substrate drive unit 141 that moves the support member 140 and the substrate 110 relative to the vessel 130. For example, the substrate drive unit 141 can translate the support member 140 (as indicated by arrow “A”) and/or rotate the support member 140 (as indicated by arrow “B”).

The apparatus 160 can further include a first electrode 120 a and a second electrode 120 b (referred to collectively as electrodes 120) supported relative to the microelectronic substrate 110 by a support member 124. In one aspect of this embodiment, the support arm 124 is coupled to an electrode drive unit 123 for moving the electrodes 120 relative to the microelectronic substrate 110. For example, the electrode drive unit 123 can move the electrodes toward and away from the conductive layer 111 of the microelectronic substrate 110, (as indicated by arrow “C”), and/or transversely.(as indicated by arrow “D”) in a plane generally parallel to the conductive layer 111. Alternatively, the electrode drive unit 123 can move the electrodes in other fashions, or the electrode drive unit 123 can be eliminated when the substrate drive unit 141 provides sufficient relative motion between the substrate 110 and the electrodes 120.

In either embodiment described above with reference to FIG. 3, the electrodes 120 are coupled to a current source 121 with leads 128 for supplying electrical current to the electrolyte 131 and the conductive layer 111. In operation, the current source 121 supplies an alternating current (single phase or multiphase) to the electrodes 120. The current passes through the electrolyte 131 and reacts electrochemically with the conductive layer 111 to remove material (for example, atoms or groups of atoms) from the conductive layer 111. The electrodes 120 and/or the substrate 110 can be moved relative to each other to remove material from selected portions of the conductive layer 111, or from the entire conductive layer 111.

In one aspect of an embodiment of the apparatus 160 shown in FIG. 3, a distance D₁ between the electrodes 120 and the conductive layer 111 is set to be smaller than a distance D₂ between the first electrode 120 a and the second electrode 120 b. Furthermore, the electrolyte 131 generally has a higher resistance than the conductive layer 111. Accordingly, the alternating current follows the path of least resistance from the first electrode 120 a, through the electrolyte 131 to the conductive layer 111 and back through the electrolyte 131 to the second electrode 120 b, rather than from the first electrode 120 a directly through the electrolyte 131 to the second electrode 120 b. Alternatively, a low dielectric material (not shown) can be positioned between the first electrode 120 a and the second electrode 120 b to decouple direct electrical communication between the electrodes 120 that does not first pass through the conductive layer 111.

One feature of an embodiment of the apparatus 160 shown in FIG. 3 is that the electrodes 120 do not contact the conductive layer 111 of the substrate 110. An advantage of this arrangement is that it can eliminate the residual conductive material resulting from a direct electrical connection between the electrodes 120 and the conductive layer 111, described above with reference to FIGS. 1 and 2. For example, the apparatus 160 can eliminate residual conductive material adjacent to the contact region between the electrodes and the conductive layer because the electrodes 120 do not contact the conductive layer 111.

Another feature of an embodiment of the apparatus 160 described above with reference to FIG. 3 is that the substrate 110 and/or the electrodes 120 can move relative to the other to position the electrodes 120 at any point adjacent to the conductive layer 111. An advantage of this arrangement is that the electrodes 120 can be sequentially positioned adjacent to every portion of the conductive layer to remove material from the entire conductive layer 111. Alternatively, when it is desired to remove only selected portions of the conductive layer 111, the electrodes 120 can be moved to those selected portions, leaving the remaining portions of the conductive layer 111 intact.

FIG. 4 is a partially schematic, side elevational view of an apparatus 260 that includes a support member 240 positioned to support the substrate 110 in accordance with another embodiment of the invention. In one aspect of this embodiment, the support member 240 supports the substrate 110 with the conductive layer 111 facing upwardly. A substrate drive unit 241 can move the support member 240 and the substrate 110, as described above with reference to FIG. 3. First and second electrodes 220 a and 220 b are positioned above the conductive layer 111 and are coupled to a current source 221. A support member 224 supports the electrodes 220 relative to the substrate 110 and is coupled to an electrode drive unit 223 to move the electrodes 220 over the surface of the support conductive layer 111 in a manner generally similar to that described above with reference to FIG. 3.

In one aspect of the embodiment shown in FIG. 4, the apparatus 260 further includes an electrolyte vessel 230 having a supply conduit 237 with an aperture 238 positioned proximate to the electrodes 220. Accordingly, an electrolyte 231 can be deposited locally in an interface region 239 between the electrodes 220 and the conductive layer 111, without necessarily covering the entire conductive layer 111. The electrolyte 231 and the conductive material removed from the conductive layer 111 flow over the substrate 110 and collect in an electrolyte receptacle 232. The mixture of electrolyte 231 and conductive material can flow to a reclaimer 233 that removes most of the conductive material from the electrolyte 231. A filter 234 positioned downstream of the reclaimer 233 provides additional filtration of the electrolyte 231 and a pump 235 returns the reconditioned electrolyte 231 to the electrolyte vessel 230 via a return line 236.

In another aspect of the embodiment shown in FIG. 4, the apparatus 260 can include a sensor assembly 250 having a sensor 251 positioned proximate to the conductive layer 111, and a sensor control unit 252 coupled to the sensor 251 for processing signals generated by the sensor 251. The control unit 252 can also move the sensor 251 relative to the substrate 110. In a further aspect of this embodiment, the sensor assembly 250 can be coupled via a feedback path 253 to the electrode drive unit 223 and/or the substrate drive unit 241. Accordingly, the sensor 251 can determine which areas of the conductive layer 111 require additional material removal and can move the electrodes 220 and/or the substrate 110 relative to each other to position the electrodes 220 over those areas. Alternatively, (for example, when the removal process is highly repeatable), the electrodes 220 and/or the substrate 110 can move relative to each other according to a pre-determined motion schedule.

The sensor 251 and the sensor control unit 252 can have any of a number of suitable configurations. For example, in one embodiment, the sensor 251 can be an optical sensor that detects removal of the conductive layer 111 by detecting a change in the intensity, wavelength or phase shift of the light reflected from the substrate 110 when the conductive material is removed. Alternatively, the sensor 251 can emit and detect reflections of radiation having other wavelengths, for example, x-ray radiation. In still another embodiment, the sensor 251 can measure a change in resistance or capacitance of the conductive layer 111 between two selected points. In a further aspect of this embodiment, one or both of the electrodes 220 can perform the function of the sensor 251 (as well as the material removal function described above), eliminating the need for a separate sensor 251. In still further embodiments, the sensor 251 can detect a change in the voltage and/or current drawn from the current supply 221 as the conductive layer 111 is removed.

In any of the embodiments described above with reference to FIG. 4, the sensor 251 can be positioned apart from the electrolyte 231 because the electrolyte 231 is concentrated in the interface region 239 between the electrodes 220 and the conductive layer 111. Accordingly, the accuracy with which the sensor 251 determines the progress of the electrolytic process can be improved because the electrolyte 231 will be less likely to interfere with the operation of the sensor 251. For example, when the sensor 251 is an optical sensor, the electrolyte 231 will be less likely to distort the radiation reflected from the surface of the substrate 110 because the sensor 251 is positioned away from the interface region 239.

Another feature of an embodiment of the apparatus 260 described above with reference to FIG. 4 is that the electrolyte 231 supplied to the interface region 239 is continually replenished, either with a reconditioned electrolyte or a fresh electrolyte. An advantage of this feature is that the electrochemical reaction between the electrodes 220 and the conductive layer 111 can be maintained at a high and consistent level.

FIG. 5 is a partially schematic, side elevational view of an apparatus 360 that directs alternating current to the substrate 110 through a first electrolyte 331 a and a second electrolyte 331 b. In one aspect of this embodiment, the first electrolyte 331 a is disposed in two first electrolyte vessels 330 a, and the second electrolyte 331 b is disposed in a second electrolyte vessel 330 b. The first electrolyte vessels 330 a are partially submerged in the second electrolyte 331 b. The apparatus 360 can further include electrodes 320, shown as a first electrode 320 a and a second electrode 320 b, each coupled to a current supply 321 and each housed in one of the first electrolyte vessels 330 a. Alternatively, one of the electrodes 320 can be coupled to ground. The electrodes 320 can include materials such as silver, platinum, copper and/or other materials, and the first electrolyte 331 a can include sodium chloride, potassium chloride, copper sulfate and/or other electrolytes that are compatible with the material forming the electrodes 320.

In one aspect of this embodiment, the first electrolyte vessels 330 a include a flow restrictor 322, such as a permeable isolation membrane formed from Teflon™, sintered materials such as sintered glass, quartz or sapphire, or other suitable porous materials that allow ions to pass back and forth between the first electrolyte vessels 330 a and the second electrolyte vessel 330 b, but do not allow the second electrolyte 330 b to pass inwardly toward the electrodes 320 (for example, in a manner generally similar to a salt bridge). Alternatively, the first electrolyte 331 a can be supplied to the electrode vessels 330 a from a first electrolyte source 339 at a pressure and rate sufficient to direct the first electrolyte 331 a outwardly through the flow restrictor 322 without allowing the first electrolyte 331 a or the second electrolyte 330 b to return through the flow restrictor 322. In either embodiment, the second electrolyte 331 b remains electrically coupled to the electrodes 320 by the flow of the first electrolyte 331 a through the restrictor 322.

In one aspect of this embodiment, the apparatus 360 can also include a support member 340 that supports the substrate 110 with the conductive layer 111 facing toward the electrodes 320. For example, the support member 340 can be positioned in the second electrolyte vessel 330 b. In a further aspect of this embodiment, the support member 340 and/or the electrodes 320 can be movable relative to each other by one or more drive units (not shown).

One feature of an embodiment of the apparatus 360 described above as reference to FIG. 5 is that the first electrolyte 331 a can be selected to be compatible with the electrodes 320. An advantage of this feature is that the first electrolyte 331 a can be less likely than conventional electrolytes to degrade the electrodes 320. Conversely, the second electrolyte 331 b can be selected without regard to the effect it has on the electrodes 320 because it is chemically isolated from the electrodes 320 by the flow restrictor 322. Accordingly, the second electrolyte 331 b can include hydrochloric acid or another agent that reacts aggressively with the conductive layer 111 of the substrate 110.

FIG. 6 is a top plan view of the microelectronic substrate 110 positioned beneath a plurality of electrodes having shapes and configurations in accordance with several embodiments of the invention. For purposes of illustration, several different types of electrodes are shown positioned proximate to the same microelectronic substrate 110; however, in practice, electrodes of the same type can be positioned relative to a single microelectronic substrate 110.

In one embodiment, electrodes 720 a and 720 b can be grouped to form an electrode pair 770 a, with each electrode 720 a and 720 b coupled to an opposite terminal of a current supply 121 (FIG. 3). The electrodes 770 a and 770 b can have an elongated or strip-type shape and can be arranged to extend parallel to each other over the diameter of the substrate 110. The spacing between adjacent electrodes of an electrode pair 370 a can be selected to direct the electrical current into the substrate 110, as described above with reference to FIG. 3.

In an alternate embodiment, electrodes 720 c and 720 d can be grouped to form an electrode pair 770 b, and each electrode 720 c and 720 d can have a wedge or “pie” shape that tapers inwardly toward the center of the microelectronic substrate 110. In still another embodiment, narrow, strip-type electrodes 720 e and 720 f can be grouped to form electrode pairs 770 c, with each electrode 720 e and 720 f extending radially outwardly from the center 113 of the microelectronic substrate 110 toward the periphery 112 of the microelectronic substrate 110.

In still another embodiment, a single electrode 720 g can extend over approximately half the area of the microelectronic substrate 110 and can have a semicircular planform shape. The electrode 720 g can be grouped with another electrode (not shown) having a shape corresponding to a mirror image of the electrode 720 g, and both electrodes can be coupled to the current source 121 to provide alternating current to the microelectronic substrate in any of the manners described above with reference to FIGS. 3-5.

FIG. 7 is a partially schematic, cross-sectional side elevational view of a portion of the substrate 110 positioned beneath the electrode 720 c described above with reference to FIG. 6. In one aspect of this embodiment, the electrode 720 c has an upper surface 771 and a lower surface 772 opposite the upper surface 771 and facing the conductive layer 111 of the substrate 110. The lower surface 772 can taper downwardly from the center 113 of the substrate 110 toward the perimeter 112 of the substrate 110 in one aspect of this embodiment to give the electrode 720 c a wedge-shaped profile. Alternatively, the electrode 720 c can have a plate-type configuration with the lower surface 772 positioned as shown in FIG. 7 and the upper surface 771 parallel to the lower surface 772. One feature of either embodiment is that the electrical coupling between the electrode 720 c and the substrate 110 can be stronger toward the periphery 112 of the substrate 110 than toward the center 113 of the substrate 110. This feature can be advantageous when the periphery 112 of the substrate 110 moves relative to the electrode 720 c at a faster rate than does the center 113 of the substrate 110, for example, when the substrate 110 rotates about its center 113. Accordingly, the electrode 720 c can be shaped to account for relative motion between the electrode and the substrate 110.

In other embodiments, the electrode 720 c can have other shapes. For example, the lower surface 772 can have a curved rather than a flat profile. Alternatively, any of the electrodes described above with reference to FIG. 6 (or other electrodes having shapes other than those shown in FIG. 6) can have a sloped or curved lower surface. In still further embodiments, the electrodes can have other shapes that account for relative motion between the electrodes and the substrate 110.

FIG. 8A is a partially schematic view of an electrode support 473 for supporting a plurality of electrodes in accordance with another embodiment of the invention. In one aspect of this embodiment, the electrode support 473 can include a plurality of electrode apertures 474, each of which houses either a first electrode 420 a or a second electrode 420 b. The first electrodes 420 a are coupled through the apertures 474 to a first lead 428 a and the second electrodes 420 b are coupled to a second lead 428 b. Both of the leads 428 a and 428 b are coupled to a current supply 421. Accordingly, each pair 470 of first and second electrodes 420 a and 420 b defines part of a circuit that is completed by the substrate 110 and the electrolyte(s) described above with reference to FIGS. 3-5.

In one aspect of this embodiment, the first lead 428 a can be offset from the second lead 428 b to reduce the likelihood for short circuits and/or capacitive coupling between the leads. In a further aspect of this embodiment, the electrode support 473 can have a configuration generally similar to any of those described above with reference to FIGS. 1-7. For example, any of the individual electrodes (e.g., 320 a, 320 c, 320 e, or 320 g) described above with reference to FIG. 6 can be replaced with an electrode support 473 having the same overall shape and including a plurality of apertures 474, each of which houses one of the first electrodes 420 a or the second electrodes 420 b.

In still a further aspect of this embodiment, the electrode pairs 470 shown in FIG. 8A can be arranged in a manner that corresponds to the proximity between the electrodes 420 a, 420 b and the microelectronic substrate 110 (FIG. 7), and/or the electrode pairs 470 can be arranged to correspond to the rate of relative motion between the electrodes 420 a, 420 b and the microelectronic substrate 110. For example, the electrode pairs 470 can be more heavily concentrated in the periphery 112 of the substrate 110 or other regions where the relative velocity between the electrode pairs 470 and the substrate 110 is relatively high (see FIG. 7). Accordingly, the increased concentration of electrode pairs 470 can provide an increased electrolytic current to compensate for the high relative velocity. Furthermore, the first electrode 420 a and the second electrode 420 b of each electrode pair 470 can be relatively close together in regions (such as the periphery 112 of the substrate 110) where the electrodes are close to the conductive layer 111 (see FIG. 7) because the close proximity to the conductive layer 111 reduces the likelihood for direct electrical coupling between the first electrode 420 a and the second electrode 420 b. In still a further aspect of this embodiment, the amplitude, frequency and/or waveform shape supplied to different electrode pairs 470 can vary depending on factors such as the spacing between the electrode pair 470 and the microelectronic substrate 110, and the relative velocity between the electrode pair 470 and the microelectronic substrate 110.

FIGS. 8B-8C illustrate electrodes 820 (shown as first electrodes 820 a and second electrodes 820 b) arranged concentrically in accordance with still further embodiments of the invention. In one embodiment shown in FIG. 8B, the first electrode 820 a can be positioned concentrically around the second electrode 820 b, and a dielectric material 829 can be disposed between the first electrode 820 a and the second electrode 820 b. The first electrode 820 a can define a complete 360° arc around the second electrode 820 b, as shown in FIG. 8B, or alternatively, the first electrode 820 a can define an arc of less than 360°.

In another embodiment, shown in FIG. 8C, the first electrode 820A can be concentrically disposed between two second electrodes 820 b, with the dielectric material 829 disposed between neighboring electrodes 820. In one aspect of this embodiment, current can be supplied to each of the second electrodes 820 b with no phase shifting. Alternatively, the current supplied to one second electrode 820 b can be phase-shifted relative to the current supplied to the other second electrode 820 b. In a further aspect of the embodiment, the current supplied to each second electrode 820 b can differ in characteristics other than phase, for example, amplitude.

One feature of the electrodes 820 described above with respect to FIGS. 8B-8C is that the first electrode 820 a can shield the second electrode(s) 820 b from interference from other current sources. For example, the first electrode 820 a can be coupled to ground to shield the second electrodes 820 b. An advantage of this arrangement is that the current applied to the substrate 110 (FIG. 7) via the electrodes 820 can be more accurately controlled.

FIG. 9 schematically illustrates an apparatus 560 for both planarizing and electrolytically processing the microelectronic substrate 110 in accordance with an embodiment of the invention. In one aspect of this embodiment, the apparatus 560 has a support table 580 with a top-panel 581 at a workstation where an operative portion “W” of a planarizing or polishing pad 582 is positioned. The top-panel 581 is generally a rigid plate to provide a flat, solid surface to which a particular section of the planarizing pad 582 may be secured during planarization.

The apparatus 560 can also have a plurality of rollers to guide, position and hold the planarizing pad 582 over the top-panel 581. The rollers can include a supply roller 583, first and second idler rollers 584 a and 584 b, first and second guide rollers 585 a and 585 b, and a take-up roller 586. The supply roller 583 carries an unused or pre-operative portion of the planarizing pad 582, and the take-up roller 583 carries a used or post-operative portion of the planarizing pad 582. Additionally, the first idler roller 584 a and the first guide roller 585 a can stretch the planarizing pad 582 over the top-panel 581 to hold the planarizing pad 582 stationary during operation. A motor (not shown) drives at least one of the supply roller 583 and the take-up roller 586 to sequentially advance the planarizing pad 582 across the top-panel 581. Accordingly, clean pre-operative sections of the planarizing pad 582 may be quickly substituted for used sections to provide a consistent surface for planarizing and/or cleaning the substrate 110.

The apparatus 560 can also have a carrier assembly 590 that controls and protects the substrate 110 during planarization. The carrier assembly 590 can include a substrate holder 592 to pick up, hold and release the substrate 110 at appropriate stages of the planarizing process. The carrier assembly 590 can also have a support gantry 594 carrying a drive assembly 595 that can translate along the gantry 594. The drive assembly 595 can have an actuator 596, a drive shaft 597 coupled to the actuator 596, and an arm 598 projecting from the drive shaft 597. The arm 598 carries the substrate holder 592 via a terminal shaft 599 such that the drive assembly 595 orbits the substrate holder 592 about an axis E-E (as indicated by arrow “R₁”). The terminal shaft 599 may also rotate the substrate holder 592 about its central axis F-F (as indicated by arrow “R₂”).

The planarizing pad 582 and a planarizing solution 587 define a planarizing medium that mechanically and/or chemically-mechanically removes material from the surface of the substrate 110. The planarizing pad 582 used in the apparatus 560 can be a fixed-abrasive planarizing pad in which abrasive particles are fixedly bonded to a suspension medium. Accordingly, the planarizing solution 587 can be a “clean solution” without abrasive particles because the abrasive particles are fixedly distributed across a planarizing or polishing surface 588 of the planarizing pad 582. In other applications, the planarizing pad 582 may be a non-abrasive pad without abrasive particles, and the planarizing solution 587 can be a slurry with abrasive particles and chemicals to remove material from the substrate 110.

To planarize the substrate 110 with the apparatus 560, the carrier assembly 590 presses the substrate 110 against the planarizing surface 588 of the planarizing pad 582 in the presence of the planarizing solution 587. The drive assembly 595 then orbits the substrate holder 592 about the axis E-E and optionally rotates the substrate holder 592 about the axis F-F to translate the substrate 110 across the planarizing surface 588. As a result, the abrasive particles and/or the chemicals in the planarizing medium remove material from the surface of the substrate 110 in a chemical and/or chemical-mechanical planarization (CMP) process. Accordingly, the planarizing pad 582 can smooth the substrate 110 by removing rough features projecting from the conductive layer 111 of the substrate 110.

In a further aspect of this embodiment, the apparatus 560 can include an electrolyte supply vessel 530 that delivers an electrolyte to the planarizing surface of the planarizing pad 582 with a conduit 537, as described in greater detail with reference to FIG. 10. The apparatus 560 can further include a current supply 521 coupled to the support table 580 and/or the top-panel 581 to supply an electrical current to electrodes positioned in the support table 580 and/or the top-panel 581. Accordingly, the apparatus 560 can electrolytically remove material from the conductive layer 111 in a manner similar to that described above with reference to FIGS. 1-8C.

In one aspect of an embodiment of the apparatus 560 described above with reference to FIG. 9, material can be sequentially removed from the conductive layer 111 of the substrate 110 first by an electrolytic process and then by a CMP process. For example, the electrolytic process can remove material from the conductive layer 111 in a manner that roughens the conductive layer 111. After a selected period of electrolytic processing time has elapsed, the electrolytic processing operation can be halted and additional material can be removed via CMP processing. Alternatively, the electrolytic process and the CMP process can be conducted simultaneously. In either of these processing arrangements, one feature of an embodiment of the apparatus 560 described above with reference to FIG. 9 is that the same apparatus 560 can planarize the substrate 110 via CMP and remove material from the substrate 110 via an electrolytic process. An advantage of this arrangement is that the substrate 110 need not be moved from one apparatus to another to undergo both CMP and electrolytic processing.

Another advantage of an embodiment of the apparatus 560 described above with reference to FIG. 9 is that the processes, when used in conjunction with each other, is expected to remove material from the substrate 110 more quickly and accurately than some conventional processes. For example, as described above, the electrolytic process can remove relatively large amounts of material in a manner that roughens the microelectronic substrate 110, and the planarizing process can remove material on a finer scale in a manner that smoothes and/or flattens the microelectronic substrate 110.

In particular embodiments, the amount of water in the electrolytic liquid (e.g., the composite mixture of the planarizing liquid 587 and the electrolyte provided by the electrolyte supply vessel 530) can be less than that of existing electrolytic liquids used for polishing and/or planarizing the microelectronic substrates 110. As described in greater detail below, a feature of these embodiments is that such a liquid can permit an operator to reduce the normal force (e.g., the downforce) applied at the interface between the microelectronic substrate 110 and the planarizing pad 582. An advantage of this arrangement is that the likelihood for breaking the microelectronic substrate 110 during processing can be reduced, the uniformity with which material is removed from the microelectronic substrate 110 can be increased, and/or the likelihood for smearing materials at the surface of the microelectronic substrate 110 can be reduced. In a particular embodiment, tantalum can be removed from the microelectronic substrate 110 at a significantly reduced downforce. For example, the downforce can be reduced from a conventional value of about 2 psi to a value of from about 0.1 psi to about 1 psi. In the limit, the downforce can be reduced to zero and the electrolytic liquid can be disposed in an apparatus generally similar to any of those described above with reference to FIGS. 3-5. Electrolytic liquids having compositions suitable for this and other embodiments are described in greater detail below.

In one embodiment, the electrolytic liquid can include a pure or nearly pure organic solvent and a dissolved salt, with an overall water content of about 1% (by volume) or less. Electrolytic liquids having water contents in this range can be less likely to passivate the conductive material of the microelectronic substrate 110. In a particular embodiment, the electrolytic liquid can include methanol and ammonium chloride. In a particular aspect of this embodiment, an electrolytic liquid having this composition can be used to electrochemically and/or electrochemically-mechanically remove tantalum and/or tantalum nitride from the microelectronic substrate 110, with a significantly reduced downforce. For example, in a further particular aspect of this embodiment, the polishing pad 582 can be eliminated and the tantalum or tantalum compound can be removed electrochemically without contact with a polishing pad. It is believed that one possible reason for the reduced down force is that the tantalum and/or tantalum nitride typically oxidizes to form a tantalum pentoxide film, which is very stable in an aqueous system. However, in an organic solvent system the tantalum pentoxide may be less stable due to the formation of tantalum-methoxide complexes (e.g., Ta—(O—CH₃)_(x)) or other metal-organic species in solution. The complexing interaction may occur directly with the tantalum and/or with the tantalum pentoxide film and may be thermodynamically more likely to occur in the presence of a pure or nearly pure organic solvent than in the presence of an aqueous system.

In one embodiment (as described above) the electrolytic liquid can include about 1% water or less. In other embodiments, the electrolytic liquid can include greater amounts of water while still allowing a reduction in the downforce applied between the microelectronic substrate 110 and the planarizing pad 582. For example, in one embodiment, the electrolytic liquid can include less than about 10% water. In other embodiments, the electrolytic liquid can include less than about 50% water or less than about 80% water. The particular amount of water (if any) selected for the electrolytic liquid can depend upon the desired reduction in downforce and/or the composition of the material to be removed from the microelectronic substrate 110.

In one embodiment (as described above) the electrolytic liquid can include an alcohol as the solvent. In other embodiments, the electrolytic liquid can include other non-aqueous polar solvents, or mixtures of organic solvents (with some polar and some not), with the overall mixture being at least partially polar. Examples of other non-aqueous polar solvents include but are not limited to organic amines (including triethylamine and/or analine), organic acids (including beta diketone and/or 2,5-pentanedione), carboxylic acids (including acetic acid and/or formic acid), nitrites (including acetonitrile), and isonitriles (including methylisonitrile). Other substances, all of which are polar to some degree, include aromatic hydrocarbons (e.g., xylene), organic phosphates (e.g., triethylphosphate), halocarbons (e.g., bromoethane) and alkoxides and/or oxo alkoxides.

In a further aspect of an embodiment described above with reference to FIG. 9, the apparatus 560 can include one or more features configured to restrict the amount of water absorbed by or otherwise mixed with the electrolytic liquid during processing. For example, in one aspect of this embodiment, the apparatus 560 can include an at least partially (and in one embodiment, completely) water-tight enclosure 501 that surrounds the electrolytic liquid on the planarizing pad 582. In one aspect of this embodiment, the enclosure 501 can include a clean room. In other embodiments, the enclosure 501 can be smaller to control an environment around only a portion of the apparatus 560. In either embodiment, the enclosure 501 can include a sealable access portion 502 (shown open in FIG. 9) to allow ingress and egress of the microelectronic substrates 110 and/or personnel required to operate the apparatus 560. A door or other sealable device 509 can be removably positioned in the access portion 502. In one aspect of this embodiment, the region within the enclosure 501 can be filled with a purge gas provided through a purge gas port 503. The purge gas can include an inert gas (e.g., nitrogen) that can displace any water vapor within the enclosure 501 without having an effect on the chemical, electrical, and/or mechanical interaction with the microelectronic substrate 110. In another embodiment, the purge gas port 503 can be coupled to a vacuum source to evacuate the environment within the enclosure 501. In either embodiment, a desiccant 504 (which can include calcium sulfate, molecular sieves, or other hydrophilic substances) can be positioned within the enclosure 501 to remove any residual water vapor within the enclosure 501. Accordingly, the amount of water (if any) in the electrolytic liquid can be controlled to preserve the associated benefits described above. In another embodiment, the desiccant can be disposed directly in the electrolytic liquid. For example, the desiccant can have abrasive properties and can accordingly aid in polishing the microelectronic substrate 110. After absorbing water, the desiccant can be filtered from the electrolyte, dehydrated and recycled. In still another embodiment, the electrolyte can be stored near the desiccant, then provided to the planarizing pad 582 for processing, and then removed for dehydrating and recycling.

FIG. 10 is a partially exploded, partially schematic isometric view of a portion of the apparatus 560 described above with reference to FIG. 9. In one aspect of an embodiment shown in FIG. 10, the top-panel 581 houses a plurality of electrode pairs 570, each of which includes a first electrode 520 a and a second electrode 520 b. The first electrodes 520 a are coupled to a first lead 528 a and the second electrodes 520 b are coupled to a second lead 528 b. The first and second leads 528 a and 528 b are coupled to the current source 521 (FIG. 9). In one aspect of this embodiment, the first electrode 520 a can be separated from the second electrodes 520 b by an electrode dielectric layer 529 a that includes Teflon™ or another suitable dielectric material. The electrode dielectric layer 529 a can accordingly control the volume and dielectric constant of the region between the first and second electrodes 520 a and 520 b to control electrical coupling between the electrodes.

The electrodes 520 a and 520 b can be electrically coupled to the microelectronic substrate 110 (FIG. 9) by the planarizing pad 582. In one aspect of this embodiment, the planarizing pad 582 is saturated with an electrolyte 531 supplied by the supply conduits 537 through apertures 538 in the top-panel 581 just beneath the planarizing pad 582. Accordingly, the electrodes 520 a and 520 b are selected to be compatible with the electrolyte 531. In an alternate arrangement, the electrolyte 531 can be supplied to the planarizing pad 582 from above (for example, by disposing the electrolyte 531 in the planarizing liquid 587) rather than through the top-panel 581. Accordingly, the planarizing pad 582 can include a pad dielectric layer 529 b positioned between the planarizing pad 582 and the electrodes 520 a and 520 b. When the pad dielectric layer 529 b is in place, the electrodes 520 a and 520 b are isolated from physical contact with the electrolyte 531 and can accordingly be selected from materials that are not necessarily compatible with the electrolyte 531.

In either of the embodiments described above with reference to FIG. 10, the planarizing pad 582 can provide several advantages over some conventional electrolytic arrangements. For example, the planarizing pad 582 can uniformly separate the electrodes 520 a and 520 b from the microelectronic substrate 110 (FIG. 9), which can increase the uniformity with which the electrolytic process removes material from the conductive layer 111 (FIG. 9). The planarizing pad 582 can also have abrasive particles 589 for planarizing the microelectronic substrate 110 in the manner described above with reference to FIG. 9. Furthermore, the planarizing pad 582 can filter carbon or other material that erodes from the electrodes 520 a and 520 b to prevent the electrode material from contacting the microelectronic substrate 110. Still further, the planarizing pad 582 can act as a sponge to retain the electrolyte 531 in close proximity to the microelectronic substrate 110.

FIG. 11 is a partially schematic, cross-sectional side elevational view of a rotary apparatus 660 for planarizing and/or electrolytically processing the microelectronic substrate 110 in accordance with another embodiment of the invention. In one aspect of this embodiment, the apparatus 660 has a generally circular platen or table 680, a carrier assembly 690, a planarizing or polishing pad 682 positioned on the table 680, and an electrolytic liquid 687 on the planarizing pad 682. The planarizing pad 682 can be a fixed abrasive planarizing pad or, alternatively, the electrolytic liquid 687 can include a slurry having a suspension of abrasive elements and the planarizing pad 682 can be a non-abrasive pad. A drive assembly 695 rotates (arrow “G”) and/or reciprocates (arrow “H”) the platen 680 to move the planarizing pad 682 during planarization.

The carrier assembly 690 controls and protects the microelectronic substrate 110 during planarization. The carrier assembly 690 typically has a substrate holder 692 with a pad 694 that holds the microelectronic substrate 110 via suction. A drive assembly 696 of the carrier assembly 690 typically rotates and/or translates the substrate holder 692 (arrows “I” and “J,” respectively). Alternatively, the substrate holder 692 may include a weighted, free-floating disk (not shown) that slides over the planarizing pad 682.

To planarize the microelectronic substrate 110 with the apparatus 660, the carrier assembly 690 presses the microelectronic substrate 110 against a planarizing surface 688 of the planarizing pad 682. The platen 680 and/or the substrate holder 692 then move relative to one another to translate the microelectronic substrate 110 across the planarizing surface 688. As a result, the abrasive particles in the planarizing pad 682 and/or the chemicals in the electrolytic liquid 687 remove material from the surface of the microelectronic substrate 110.

The apparatus 660 can also include a current source 621 coupled with leads 628 a and 628 b to one or more electrode pairs 670 (one of which is shown in FIG. 11). The electrode pairs 670 can be integrated with the platen 680 in generally the same manner with which the electrodes 520 a and 520 b (FIG. 10) are integrated with the top panel 581 (FIG. 10). Alternatively, the electrode pairs 670 can be integrated with the planarizing pad 682. In either embodiment, the electrode pairs 670 can include electrodes having shapes and configurations generally similar to any of those described above with reference to FIGS. 3-10 to electrolytically remove conductive material from the microelectronic substrate 110. The electrolytic process can be carried out before, during or after the CMP process, as described above with reference to FIG. 9.

In one aspect of an embodiment of the apparatus 660 described above with reference to FIG. 11, an enclosure 601 can be disposed around the planarizing pad 682 and the electrolytic liquid 687 to control the amount of water (if any) that mixes with the electrolytic liquid 687. In another aspect of this embodiment, the apparatus 660 can include a fluid collector 605 positioned to collect the electrolytic liquid 687 as it flows off the planarizing pad 682. The electrolytic liquid 687 can pass through a return conduit 606 to a pump 607 which returns the electrolytic liquid 687 to the planarizing pad 682 via a supply conduit 609. A separator 608 can be positioned at a selected point along the return conduit 606 and/or the supply conduit 609 to remove some or all of any water that may become a constituent of the electrolytic liquid 687. The separator 608 can be used in addition to or in lieu of the desiccant and/or purge gas described above with reference to FIG. 9.

In one aspect of an embodiment of the apparatus 660 shown in FIG. 11, all the liquid disposed on the planarizing pad 682 can be provided by a single supply conduit. Accordingly, the liquid provided by the supply conduit 609 can have both electrolytic characteristics and planarizing/polishing characteristics. For example, in one aspect of this embodiment, the liquid can include a suspension of abrasive elements. In other embodiments, liquids having electrolytic characteristics can be mixed at the planarizing pad 687 with liquids having polishing characteristics, for example, in a manner generally similarly to that described above with reference to FIG. 9. In either embodiment, the region adjacent to the planarizing pad 687, including the region between the planarizing pad 687 and the microelectronic substrate 110, can define an electrolytic liquid volume 611, which receives electrolytic liquid and in which the microelectronic substrate 110 is electrolytically processed.

FIG. 12A is a schematic circuit representation of some of the components described above with reference to FIG. 10. The circuit analogy can also apply to any of the arrangements described above with reference to FIGS. 3-11. As shown schematically in FIG. 12A, the current source 521 is coupled to the first electrode 520 a and the second electrode 520 b with leads 528 a and 528 b respectively. The electrodes 520 a and 520 b are coupled to the microelectronic substrate 110 with the electrolyte 531 in an arrangement that can be represented schematically by two sets of parallel capacitors and resistors. A third capacitor and resistor schematically indicates that the microelectronic substrate 110 “floats” relative to ground or another potential.

In one aspect of an embodiment shown in FIG. 12A, the current source 521 can be coupled to an amplitude modulator 522 that modulates the signal produced by the current source 521, as is shown in FIG. 12B. Accordingly, the current source 521 can generate a high-frequency wave 804, and the amplitude modulator 522 can superimpose a low-frequency wave 802 on the high-frequency wave 804. For example, the high-frequency wave 804 can include a series of positive or negative voltage spikes contained within a square wave envelope defined by the low-frequency wave 802. Each spike of the high-frequency wave 804 can have a relatively steep rise time slope to transfer charge through the dielectric to the electrolyte, and a more gradual fall time slope. The fall time slope can define a straight line, as indicated by high-frequency wave 804, or a curved line, as indicated by high-frequency wave 804 a. In other embodiments, the high-frequency wave 804 and the low-frequency wave 802 can have other shapes depending, for example, on the particular characteristics of the dielectric material and electrolyte adjacent to the electrodes 420, the characteristics of the substrate 110, and/or the target rate at which material is to be removed from the substrate 110.

An advantage of this arrangement is that the high frequency signal can transmit the required electrical energy from the electrodes 520 a and 520 b to the microelectronic substrate 110, while the low frequency superimposed signal can more effectively promote the electrochemical reaction between the electrolyte 531 and the conductive layer 111 of the microelectronic substrate 110. Accordingly, any of the embodiments described above with reference to FIGS. 3-11 can include an amplitude modulator in addition to a current source.

From the foregoing, it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims. 

1. An apparatus for removing material from a microelectronic substrate, comprising: an electrolytic liquid volume coupleable to a supply of electrolytic liquid; a carrier positioned to releasably carry a microelectronic substrate having a metal layer in fluid communication with the electrolytic liquid volume, the electrolytic liquid volume being selected to have a solvent such that a metal-oxide compound of the metal layer is less stable in the electrolytic liquid volume than in an aqueous solution; an enclosure disposed substantially completely around the electrolytic liquid volume and the carrier, the enclosure being configured to at least restrict passage of water from a region external of the enclosure to a region internal of the enclosure; and a desiccant positioned in the enclosure, the desiccant being configured to remove water vapor from the region internal of the enclosure.
 2. The apparatus of claim 1 wherein the enclosure is coupled to a source of non-aqueous purge gas.
 3. The apparatus of claim 1, further comprising a support member configured to carry a polishing pad.
 4. The apparatus of claim 1, further comprising: a support member configured to carry a polishing pad; and a polishing pad carried by the support member.
 5. The apparatus of claim 1, further comprising a support member configured to carry a generally round polishing pad.
 6. The apparatus of claim 1, further comprising: a support member configured to carry an elongated polishing pad; a first roller configured to carry an unused portion of the polishing pad; and a second roller configured to carry a used portion of the polishing pad.
 7. The apparatus of claim 1, further comprising: a polishing pad; and an electrolytic liquid adjacent to the polishing pad, wherein the electrolytic liquid includes an organic solvent.
 8. The apparatus of claim 1, further comprising: a polishing pad; and an electrolytic liquid adjacent to the polishing pad, wherein the electrolytic liquid includes about 10% water or less.
 9. An apparatus for removing material from a microelectronic substrate, comprising: an electrolytic liquid that includes a non-aqueous polar solvent; a carrier configured to releasably carry a microelectronic substrate having a metal layer in fluid communication with the electrolytic liquid, wherein the non-aqueous polar solvent is selected such that a metal-oxide compound of the metal layer is less stable in the electrolytic liquid than in an aqueous solution; a polishing pad support; a polishing pad carried by the polishing pad support, the polishing pad being positioned to contact a microelectronic substrate carried by the carrier; an enclosure disposed generally completely around the electrolytic liquid, the carrier, the polishing pad support, and the polishing pad, the enclosure being configured to at least restrict passage of water from a region external of the enclosure to a region internal of the enclosure; and a desiccant positioned in the enclosure, the desiccant being configured to remove water vapor from the region internal of the enclosure.
 10. The apparatus of claim 9 wherein the electrolytic liquid includes about 80% water or less.
 11. The apparatus of claim 9 wherein the electrolytic liquid includes about 1% water or less.
 12. The apparatus of claim 9 wherein the electrolytic liquid includes an organic solvent and a salt.
 13. The apparatus of claim 9 wherein the electrolytic liquid includes methanol.
 14. The apparatus of claim 9 wherein the electrolytic liquid includes ammonium chloride.
 15. An apparatus for removing material from a microelectronic substrate, comprising: an electrolytic liquid having a solvent that is essentially free of water; a carrier configured to releasably carry a microelectronic substrate having a tantalum layer in fluid communication with the electrolytic liquid, wherein the solvent of the electrolytic liquid is selected such that a tantalum oxide compound is less stable in the electrolytic liquid than in an aqueous solution; a polishing pad support; a polishing pad carried by the polishing pad support, the polishing pad being positioned to contact the microelectronic substrate carried by the carrier; an enclosure disposed generally completely around the electrolytic liquid, the carrier, the polishing pad support, and the polishing pad, the enclosure being configured to at least restrict passage of water from a region external of the enclosure to a region internal of the enclosure; and a desiccant positioned in the enclosure, the desiccant being configured to remove water vapor from the region internal of the enclosure.
 16. The apparatus of claim 15 wherein the electrolytic liquid includes a non-aqueous polar solvent.
 17. The apparatus of claim 15 wherein the electrolytic liquid includes an organic solvent and a salt.
 18. The apparatus of claim 15 wherein the electrolytic liquid includes methanol.
 19. The apparatus of claim 15 wherein the electrolytic liquid includes ammonium chloride. 